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rs281865069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281865069(C;G)
Make rs281865069(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position154571724
GeneCHRNB2
is asnp
is mentioned by
dbSNPrs281865069
ebirs281865069
HLIrs281865069
Exacrs281865069
Varsomers281865069
Maprs281865069
PheGenIrs281865069
hapmaprs281865069
1000 genomesrs281865069
hgdprs281865069
ensemblrs281865069
gopubmedrs281865069
geneviewrs281865069
scholarrs281865069
googlers281865069
pharmgkbrs281865069
gwascentralrs281865069
openSNPrs281865069
23andMers281865069
23andMe allrs281865069
SNP Nexus

SNPshotrs281865069
SNPdbers281865069
MSV3drs281865069
GWAS Ctlgrs281865069
Max Magnitude0
ClinVar
Risk rs281865069(G;G)
Alt rs281865069(G;G)
Reference rs281865069(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene CHRNB2
CLNDBN Epilepsy, nocturnal frontal lobe, type 3
Reversed 0
HGVS NC_000001.10:g.154544200C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000033931.2,